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Engrailed-2 and inflammation convergently and independently impinge on cerebellar Purkinje cell differentiation

2024 . Bahaaeldin, Mohammed | Bülte, Carolin | Luelsberg, Fabienne | Kumar, Sujeet | Kappler, Joachim | Völker, Christof | Schilling, Karl | Baader, Stephan L.

CK2 activity is crucial for proper glucagon expression

2024 . , | Pack, Mandy | Wrublewsky, Selina | Boewe, Anne S. | Spigelman, Aliya F. | Koch, Hanna | MacDonald, Patrick E. | Laschke, Matthias W. | Montenarh, Mathias | Götz, Claudia

Molecular subgroups of T-cell acute lymphoblastic leukemia in adults treated according to pediatric-based GMALL protocols

Panel-based RNA fusion sequencing improves diagnostics of pediatric acute myeloid leukemia

2023 . Hoffmeister, Lina Marie | Suttorp, Julia | Walter, Christiane | Antoniou, Evangelia | Behrens, Yvonne Lisa | Göhring, Gudrun | Awada, Amani | von Neuhoff, Nils | Reinhardt, Dirk | Schneider, Markus

Currarino syndrome: a comprehensive genetic review of a rare congenital disorder

2021 . Dworschak, Gabriel | Reutter, Heiko M. | Ludwig, Michael

Dysregulated paired related homeobox 1 impacts on hepatocellular carcinoma phenotypes

2021 . Piorońska, Weronika | Nwosu, Zeribe Chike | Han, Mei | Büttner, Michael | Ebert, Matthias Philip | Dooley, Steven | Meyer, Christoph

Converting fibroblastic fates leads to wound healing without scar

2021 . Jiang, Dongsheng | Rinkevich, Yuval

Genome sequencing in families with congenital limb malformations

Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update

2021 . Schätzl, Teresa | Kaiser, Lars | Deigner, Hans-Peter

Microbiota changes associated with ADNP deficiencies: rapid indicators for NAP (CP201) treatment of the ADNP syndrome and beyond

2020 . Kapitansky, Oxana | Giladi, Eliezer | Jaljuli, Iman | Bereswill, Stefan | Heimesaat, Markus M. | Gozes, Illana

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